Pharma Operations Readiness Coordinator – Onsite Strasbourg

Meet Life Sciences

Grand Est

Sur place

EUR 45 000 - 65 000

Plein temps

14 jours+
Générateur de candidature

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Résumé du poste

Meet Life Sciences is seeking a Freelance Operational Readiness Project Coordinator for pharmaceutical manufacturing in Strasbourg. You will track actions, maintain the project schedule in MS Project, and ensure alignment between the project team and operational stakeholders.

You will work onsite five days a week, coordinating cross-functional deliverables, documenting progress, and driving actions to completion in a GMP environment.

Qualifications

  • Experience coordinating pharmaceutical manufacturing projects.
  • Proficient in MS Project and project scheduling.
  • Experience maintaining schedules and cross-functional deliverables.
  • Good understanding of GMP environments.
  • Strong stakeholder management and communication abilities.
  • Ability to proactively follow up and drive actions to completion.

Responsabilités

  • Identify and capture production and operational requirements.
  • Track actions through to completion.
  • Maintain and update the operational project schedule using MS Project.
  • Interface between the project team and operational stakeholders to align schedules and needs.
  • Coordinate follow-up activities and ensure key actions stay on track.
  • Collaborate with subject matter experts to drive required documentation.
  • Monitor milestones, dependencies, and outstanding deliverables.

Connaissances

Microsoft Project
Project coordination
Stakeholder management
GMP knowledge
Communication
Organisational skills

Description du poste

Meet Life Sciences is seeking a Freelance Operational Readiness Project Coordinator for pharmaceutical manufacturing in Strasbourg. You will track actions, maintain the project schedule in MS Project, and ensure alignment between the project team and operational stakeholders.

You will work onsite five days a week, coordinating cross-functional deliverables, documenting progress, and driving actions to completion in a GMP environment.

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